Associated Papers
Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.
Lemire G et al.
American Journal of Medical Genetics. Part A, 2021
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update.
Herlin MK et al.
Orphanet Journal of Rare Diseases, 2020
Type II enteropathy-associated T-cell lymphoma features a unique genomic profile with highly recurrent SETD2 alterations.
Roberti A et al.
Nature Communications, 2016
27600764 (PubMed )
Supplement: ncomms12602-s2.xlsx › Supplementary_Data_2
Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Waschk DE et al.
Clinical Genetics, 2016
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